Canonical Allele Identifier: CA2793087686

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178806_89178811del , CM000673.2:g.89178806_89178811del	GRCh38
NC_000011.9:g.88911974_88911979del , CM000673.1:g.88911974_88911979del	GRCh37
NC_000011.8:g.88551622_88551627del	NCBI36
NG_008748.1:g.5935_5940del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+34_819+39del MANE Select	ENSP00000263321.4:n.819+34_819+39del
ENST00000263321.5:c.819+34_819+39del	ENSP00000263321.4:n.819+34_819+39del
ENST00000526139.1:n.880+34_880+39del
NM_000372.4:c.819+34_819+39del	NP_000363.1:n.819+34_819+39del
XM_011542970.1:c.819+34_819+39del	XP_011541272.1:n.819+34_819+39del
XM_011542970.2:c.819+34_819+39del	XP_011541272.1:n.819+34_819+39del
XR_001748321.1:n.2718-65278_2718-65273del
XR_001748322.1:n.2733-65278_2733-65273del
NM_000372.5:c.819+34_819+39del MANE Select	NP_000363.1:n.819+34_819+39del